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Severity of chronic experimental Chagas heart disease parallels tumournecrosis factor and nitric oxide levels in the serum: models of mild and severedisease

机译:慢性实验性恰加斯病的严重程度与肿瘤相似血清中的坏死因子和一氧化氮水平:轻度和重度模型疾病

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摘要

Heart tissue inflammation, progressive fibrosis and electrocardiographic alterations occur in approximately 30% of patients infected by Trypanosoma cruzi, 10-30 years after infection. Further, plasma levels of tumour necrosis factor (TNF) and nitric oxide (NO) are associated with the degree of heart dysfunction in chronic chagasic cardiomyopathy (CCC). Thus, our aim was to establish experimental models that mimic a range of parasitological, pathological and cardiac alterations described in patients with chronic Chagas’ heart disease and evaluate whether heart disease severity was associated with increased TNF and NO levels in the serum. Our results show that C3H/He mice chronically infected with the Colombian T. cruzi strain have more severe cardiac parasitism and inflammation than C57BL/6 mice. In addition, connexin 43 disorganisation and fibronectin deposition in the heart tissue, increased levels of creatine kinase cardiac MB isoenzyme activity in the serum and more severe electrical abnormalities were observed in T. cruzi-infected C3H/He mice compared to C57BL/6 mice. Therefore, T. cruzi-infected C3H/He and C57BL/6 mice represent severe and mild models of CCC, respectively. Moreover, the CCC severity paralleled the TNF and NO levels in the serum. Therefore, these models are appropriate forstudying the pathophysiology and biomarkers of CCC progression, as well as fortesting therapeutic agents for patients with Chagas’ heart disease.
机译:感染后10-30年,约30%的克氏锥虫感染患者发生心脏组织炎症,进行性纤维化和心电图改变。此外,血浆坏死因子(TNF)和一氧化氮(NO)的水平与慢性Chagasic心肌病(CCC)的心脏功能障碍程度相关。因此,我们的目标是建立能够模拟慢性恰加斯病患者描述的一系列寄生虫,病理和心脏改变的实验模型,并评估心脏病的严重程度是否与血清中TNF和NO水平升高有关。我们的结果表明,与C57BL / 6小鼠相比,长期感染哥伦比亚克鲁维酵母菌株的C3H / He小鼠具有更严重的心脏寄生和炎症。此外,与C57BL / 6小鼠相比,在克鲁氏衣原体感染的C3H / He小鼠中观察到心脏组织中的连接蛋白43分解和纤连蛋白沉积,血清中肌酸激酶心脏MB同工酶水平的升高以及更严重的电异常。因此,克氏锥虫感染的C3H / He和C57BL / 6小鼠分别代表严重和轻微的CCC模型。此外,CCC严重程度与血清中的TNF和NO水平平行。因此,这些模型适用于研究CCC进展的病理生理学和生物标志物,以及为Chagas心脏病患者测试治疗药物。

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